Canonical Allele Identifier: CA136868053
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1131118
gnomAD v4: 6-31271331-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271331T>G , CM000668.2:g.31271331T>G GRCh38
NC_000006.11:g.31239108T>G , CM000668.1:g.31239108T>G GRCh37
NC_000006.10:g.31347087T>G NCBI36
NG_029422.2:g.5801A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.361A>C MANE Select ENSP00000365402.5:p.Arg121=
ENST00000376228.9:c.361A>C ENSP00000365402.5:p.Arg121=
ENST00000376237.8:c.344A>C ENSP00000365412.4:p.Glu115Ala
ENST00000383329.7:c.361A>C ENSP00000372819.3:p.Arg121=
ENST00000415537.1:c.359A>C
ENST00000484378.1:n.630A>C
ENST00000487245.5:n.720A>C
ENST00000495835.1:n.550A>C
NM_002117.5:c.361A>C NP_002108.4:p.Arg121=
NM_002117.6:c.361A>C MANE Select NP_002108.4:p.Arg121=